Compounds from Agathis dammara exert hypoglycaemic activity by enhancing glucose uptake: lignans, terpenes and others

In this study, two new kaurane diterpenes (16, 17), together with 12 lignans (1–12), a triterpene (15), and two other compounds (13, 14) were isolated from the woods of Agathis dammara. The structure of the new compound was determined by HR ESIMS and 1D/2D NMR spectroscopy, and its absolute configuration was determined by electronic circular dichroism (ECD) exciton chirality method. Compounds 5, 11, 14 exhibit significant hypoglycaemic activity in zebrafish, and their mechanism of action is to enhance glucose uptake in zebrafish. Graphical Abstract Supplementary Information The online version contains supplementary material available at 10.1007/s13659-024-00440-4.


Introduction
Agathis dammara (Lamb.)Rich is a kind of arbor in the family Araucariaceae and the genus Agathis [1].The origin of A. dammara is Malaysia and the Philippines, and it has been introduced to Xiamen, Quanzhou, Fuzhou and other places in China [1].The trunk of A. dammara is rich in resin, which is widely used in industry and medicine [2].Malaysians use this resin to treat a variety of complex and inflammation-related ailments including arthritis, headaches, muscle pain, burns, fever, diarrhoea, abdominal pain [3].Related studies have shown that A. dammara has potential activities of hypoglycaemic, hypolipidemic, antioxidant, anti-inflammatory [2].In our parallel study, we found that the total diterpene component of A. dammara and its rich monomeric compound, araucarone could effectively mitigate the inflammatory response in vascular smooth muscle cells, and consequently impede the progression of abdominal aortic aneurysm through suppressing NF-kappaB/NLRP3 pathway activation [4].In the current study, two new kaurane diterpenes (16,17), together with 12 lignans (1-12), a triterpene (15), and two other compounds (13,14) were isolated from the woods of A. dammara (Fig. 1).Presented herein are the isolation, structure identification, hypoglycaemic biological evaluation and biological mechanism studies of these compounds.
By comparison the 13 C-NMR signals of 17 and 16, the difference between them leis in A ring.The C-3 position changed from a hydroxyl connected methine to a carbonyl, which shifted from δ C 82.8 to δ C 201.0.In addition, the -CH 2 CH(OH)-moiety at C-1, 2 position of 16 with signals at δ C 53.2, 210.7 changes to a hydroxyl connected alkene double bone (δ C 128.4 and 144.3) to form an α,βunsaturated ketone structure.on the aids of HSQC, COSY and HMBC, the planar structure could be established as shown in Fig. 2A.The comparison of NOE correlations (Fig. 2B), optical rotation, ECD spectrum and calculated value showed that the absolute configuration of 17 is consistent with 16 (Fig. 2C).

Study of hypoglycaemic activity of representative compounds
The zebrafish (Danio rerio) has similar glucose metabolism pathways and metabolites with those of humans, which made it an ideal model for studying the hypoglycaemic activity of drugs [18,19].In this study, a Tg (Ins:htBid TE−ON ;LR) pancreatic β cells ablation zebrafish model was used to induce hyperglycaemic symptoms [20].In the transgenic zebrafish, the truncated human Bid protein (htBid) was derived by an insulin promoter and controlled under the tetracycline-and ecdysoneinducible system.After induction with doxycycline (Dox) and tebufenozide (Tbf ), the proapoptotic tBid expression in β cells resulted in the apoptosis of β cells, which were labelled by the transgenic line Tg (− 1.2ins:H2Bmcherry).
Inhibitory of blood glucose elevation mainly includes two mechanisms in different tissues: promotion of glucose uptake in peripheral tissue and regeneration of pancreatic β cells.Two zebrafish modes were applied to reveal the hypoglycemic mechanism.
Double transgenic zebrafish Tg (Ins:htBid TE−ON ; LR); Tg (Ins:H2Bmcherry) was applied to monitor the number of β cells after the treatment of compounds.The Tg (Ins:H2Bmcherry) zebrafish pulls red fluorescent protein (mCherry) to be expressed in the β cells under the regulation of an insulin-specific promoter and is used to label the β cells.Therefore, zebrafish pancreatic β cells can be observed, statistically and imaged through fluorescence microscopy [19].Compared with the β cells ablation group (tBid + Dox + Tbf + DMSO), the number of pancreatic β cells in the hyperglycaemic zebrafish model did not change after 24 h of treatment with compounds 5, 11, 14 (Fig. 3C).This suggests that the hypoglycaemic activity of 5, 11, 14 is independent of pancreatic β cell regeneration.
Then we use the 2-NBDG, a glucose fluorescence analogue, was added in the zebrafish culture medium for indication of glucose uptake [21].Experimental results show that compounds 5, 11, 14 can significantly increase the uptake of 2-NBDG in hyperglycaemic zebrafish, with similar activity of the positive drug rosiglitazone (RGZ).This indicates that compounds 5, 11, 14 can enhance the blood glucose uptake ability of hyperglycaemic zebrafish, which is the mechanism they exert hypoglycaemic activity (Fig. 3D).

Plant material
Dried wood of Agathis dammara (Lamb.)Rich was obtain from Xiamen Garden Botanical Garden (24° 26′ 54.6ʺ N 118° 06′ 26.4ʺ E) in March 2021, Xiamen, Fujian Province, China.A voucher specimen (2021BKS) was preserved in School of Pharmaceutical Sciences, Xiamen University, and identified by Associate Professor Quan-Cheng Chen.

Extraction and isolation
A total of 1 kg of dried A. dammara wood was extracted and refluxed for 3 times with 2 L of 95% ethanol for 1.5 h to concentrate to obtain 367 g of extract, which was suspended in water and then extracted with the same volume of dichloromethane to obtain 100 g of dichloromethane extract (Fr.A), first separated by silica gel column (petroleum ether-ethyl acetate 100:1-0:1), divided into 7 components (Fr.A1-Fr.A7).
After HPLC-DAD and TLC analysis, the scheme for further separation of Fr.A2-Fr.A6 was determined, that is, off-line separation by combining reversed-phase and normal-phase open chromatographic columns, combined with preparative HPLC.Each component was firstly passed through Chromatorex C 18 as the chromatographic stationary phase, and carried out gradient elution using the conditions explored by HPLC analysis (MeOH-Water 5-100%).The eluted components were analyzed by TLC, using dichloromethane and methanol as developing solvents, and using a developing solvent formula with an Rf value of 0.2-0.3 on TLC as the mobile phase for silica gel column chromatography separation.The purity of the components separated at this time was checked by TLC and HPLC, and if impure, they were further purified by preparative HPLC (Additional file 1: Fig. S1).

ECD calculations
Conformational analyses were performed by Schrodinger Maestro 12.8 using Conformational Search function.The output conformers were then optimized at OPLS4 force field and filtered by RMSD threshold of 0.1 Å and energy window of 5.02 kcal/mol.The conformations calculated according to the Boltzmann equation at room temperature accounted for less than 1% were removed, and the five conformations with the energy closest to the lowest energy conformation were screened to calculate the excitation spectrum.The theoretical calculations were carried out using Gaussian 09W.The chosen conformers were finally optimized at B3LYP/6-31G(d) in methanol.
The ECD calculations of the chosen conformers were executed in methanol with Time-dependent Density functional theory (TD-DFT) at B3LYP/6-31 + G(d) or B3LYP/6-311 + G(d,p) level by Gaussian 09W.Rotatory strengths for 20 or 30 excited states were calculated.Finally, GaussView 6.0 was used to add the spectrum according to the energy of various conformations according to the Boltzmann energy equation to obtain the ECD calculation spectrum.

Establishment and treatment of hyperglycemic zebrafish model
Fertilized eggs of zebrafish strain Tg (Ins:htBid TE−ON , Ins:H2Bmcherry) were collected the next day, and this time was recorded as day 0 post fertilization (0 dpf ).Tbf (3 μL, 50 mmol/L) and Dox (3 μL, 100 mmol/L) were added into a 3.5 cm cell culture dish containing 6 mL 0.3 × Danieau's buffer.Then, the dish was placed in a zebrafish incubator without light for 48 h to induce β cells in 2 dpf ablation.Diabetic zebrafish that were ready to be used in experiments after β cells ablation were rinsed with 0.3 × Danieau's buffer to remove Tbf and Dox.The larvae were placed into a 24-well plate at a density of 10 zebrafishes/well, in 2 mL of egg water.All compounds were made in 10 mM with DMSO (prepare other concentrations when calculating ED 50 ).For the treatment, each group was added accordingly with 2 mL of egg water treated with 1 μL of each of the compounds (10 mmol/L) to reach the final concentration of (5 μmol/L), and the control group was treated with the same amount of DMSO.The treatments lasted for 24 h in the zebrafish incubator.The group of tBid which was not induced with Tbf and Dox was used as a control of normal zebrafish.

Total glucose level test
After the compound treatment, a pool of 10 larvae was homogenized in 100 μL of sample buffer.The homogenate was spun at 10,000 rpm for 10 min.Free glucose in 10 μL of supernatant (equivalent of one larva) was determined according to the manufacturer's instructions.Fluorescence (excitation, 520 nm; emission, 580-640 nm) was measured using a SpectraMax M5 Microplate Reader (Molecular Devices, California, USA).Each sample was measured for three pools.The obtained data were imported into GraphPad Prism 8.0.2 software, and the statistical differences among the groups were analyzed using the t-test method.

2-NBDG test
After the compound treatment, zebrafish (6 dpf ) were incubated in a culture medium containing 600 μmol/L 2-NBDG (Apexbio, B6035, Texas, USA) for 3 h.A pool of 5 larvae was homogenized in 100 μL of sample buffer.The homogenate was spun at 10,000 rpm for 10 min.The supernatant (30 μL) was placed into a 96-well plate to detect fluorescence (excitation, blue 475 nm; emission, 500-550 nm) using a SpectraMax M5 Microplate Reader (Molecular Devices, California, USA).Each sample was measured for three pools.The obtained data were imported into GraphPad Prism 8.0.2 software, and the statistical differences among the groups were analyzed using the ordinary one-way (ANOVA) method.

Microscopic imaging and counting of pancreatic cells
The compounds with 0.3 × Danieau's buffer were washed out after the compound treatment in 24 h.The larvae with 4% paraformaldehyde were fixed overnight at 4 °C and placed on a slide with aqua-mount (Richard-AllanScientific, Michigan, USA) with the right sides of the larvae facing up to expose the islets.The number of cells number was counted according to the RFP and GFP under a Leica TCS SP8 microscope (Leica, Weztlar, Germany) with 63 × lens.Microscopic images were processed and counted by LASX Office 1.4.5 software.The obtained data were imported into GraphPad Prism 8.0.2 software, and the statistical differences among the groups were analyzed using the ordinary one-way (ANOVA) method.

Conclusion
In summary, two new kaurane diterpenes (3β)-3,13dihydroxykaur-16-en-2-one (16) and 2,13-dihydroxykaura-1,16-dien-3-one (17) along with 15 known compounds were isolated from the woods of A. dammara.Among them, three compounds 5, 11, and 14 showed significant hypoglycaemic activity in the hyperglycaemic zebrafish model.Further mechanism analysis showed that this activity was caused by improving the glucose uptake ability of zebrafish.These findings enrich the structural diversity of diterpenes from the genus Agathis and provide potential lead compounds for the development of naturally derived antihyperglycemic drugs.

Fig. 2
Fig. 2 Structural elucidation of compounds 16, 17.A COSY and key HMBC signals.B NOESY correlations and relative configurations.C ECD spectral of 16, 17 versus calculated values

Fig. 3
Fig. 3 Biological evaluation and mechanism study of the hypoglycaemic activity of isolated compounds.A Blood glucose value of hyperglycaemic zebrafish model after treatment with compounds 1-17 for 24 h.B ED 50 value calculation of the hypoglycaemic activity of compounds 5, 11, 14.C Changes in the number of pancreatic β cells in the hyperglycaemic zebrafish model after treatment with compounds 5, 11, 14 for 24 h.D Changes in the 2-NBDG uptake ability of the hyperglycaemic zebrafish model after treatment with compounds 5, 11, 14 for 24 h.(*p < 0.05; **p < 0.01; ***p < 0.001)